Zobrazeno 1 - 10 of 13 pro vyhledávání: '"Miburge Bolivar Gois"'
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Akademický článek
Prevalência de hipertensão, cardiopatias e fatores de risco em amostra populacional na cidade de Aracaju/SE
Autor: Miburge Bolivar Gois Junior, Giulliani Antonicelli Moreira Brasileiro, Elenilton Correia de Souza, Luan Phillipe Moreira Cândido, José Aislan Correia Santos, Diogo Costa Garção, Karina Conceição Gomes Machado de Araújo
Publikováno v: Revista de Educação Física, Vol 88, Iss 1 (2019)
Introdução: Doenças cardiovasculares são a principal causa de mortalidade, no Brasil e no mundo. Estudos em amostra populacional brasileira, fatores de risco para o desenvolvimento de doenças cardiovasculares são escassos. Objetivo: Estimar a p
Externí odkaz: https://doaj.org/article/11e01a972cda459b9c98c1c91a00071a
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4
Postural phenotype assessment in pupils: a new clinic approach
Autor: Flávio Nascimento Filho, Luana Karina Almeida Nascimento, Maria das Graças Rodrigues de Araújo, Cristiano Barreto de Miranda, Miburge Bolivar Gois Junior, Felipe Cerqueira
Publikováno v: Manual Therapy, Posturology & Rehabilitation Journal. :1-7
Introduction: Most of the postural problems originate during puberty, when the body structure is in the process of development and the hormonal release predisposes the differentiated growth between the gender, which can interfere in the posture and b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::efc300fe0396f1fe838aebde5ef98c8a
https://doi.org/10.17784/mtprehabjournal.2016.14.390
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5
Effect of manipulation by maitland method in the treatment of adhesive capsulitis of the shoulder: case studies
Autor: Maria de Fátima Alcântara Barros, Vivianne Camila de Souza Bastos, Maria das Graças Rodrigues de Araújo, Antonio Geraldo Cidrão de Carvalho, Marcelo Renato Guerino, Miburge Bolivar Gois Junior, Mafra Raiele Torres Oliveira, Shirley Lima Campos, Lívia Shirahige Gomes do Nascimento
Publikováno v: Manual Therapy, Posturology & Rehabilitation Journal. :1-6
Introduction: Adhesive capsulitis, also called frozen shoulder, affects about 3-5% of the population, especially in the age group 40 to 60 years, affecting more women and having an insidious onset. Objective: Analyze the isolated effect of joint mani
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e934b60906eec15d5282baff753286f8
https://doi.org/10.17784/mtprehabjournal.2016.14.427
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6
Síndrome de Seckel: relato de caso de recuperação motora funcional utilizando facilitação neuromuscular proprioceptiva / Método de Kabat
Autor: Jeferson de Lima Souza, Miburge Bolivar Gois Júnior, Diogo Costa Garção, Elenilton Correia de Souza, Isaac Rafael Silva Lima, Olga Sueli Marques Moreira
Publikováno v: Research, Society and Development; Vol. 11 No. 2; e37111225080
Research, Society and Development; Vol. 11 Núm. 2; e37111225080
Research, Society and Development; v. 11 n. 2; e37111225080
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Introduction: Seckel syndrome (SCKL) is a heterogeneous autosomal recessive disorder, the major characteristic of which is microcephalic osteodysplastic dwarfism, which is defined as severe intrauterine growth retardation, severe short stature, sever
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eda433c273d365b8f6a3c78eb27b7cd6
https://doi.org/10.33448/rsd-v11i2.25080
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9
Heterozygosity for a Mutation in the Growth Hormone-Releasing Hormone Receptor Gene Does Not Influence Adult Stature, But Affects Body Composition
Autor: Tábita A. R. Vicente, Joselina Luzia Menezes Oliveira, Ívina E. S. Rocha, José Augusto Barreto-Filho, Manuel H. Aguiar-Oliveira, Francielle T. Oliveira, Catarine T. Farias, Viviane C. Campos, Rossana M. C. Pereira, Celi Marques-Santos, Roberto Salvatori, Alessia Sagazio, Carla R. P. Oliveira, Miburge Bolivar Gois
Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 92:2353-2357
Context: Biallelic mutations in the GHRH receptor (GHRHR) gene (GHRHR) are a frequent cause of isolated GH deficiency (IGHD). Although heterozygous carriers of these mutations appear normal, we hypothesized that heterozygosity for a GHRHR mutation mi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ed90b2ced0d35d47314bfd8a0a262c6
https://doi.org/10.1210/jc.2007-0092
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